An Observational Study of Epoetin Beta (NeoRecormon) in Participants With Cancer Receiving Chemotherapy

Hoffmann-La Roche1,167 enrolled

Overview

This observational study will evaluate the efficacy and safety of epoetin beta (NeoRecormon) in participants with symptomatic anemia and cancer receiving chemotherapy. Participants receiving NeoRecormon once weekly in accordance with the Summary of Product Characteristics will be followed for 4 months.

Study Type

OBSERVATIONAL

Enrollment

1,167

Conditions

Anemia

Interventions

Epoetin betaDRUG

Treatment will be given according to standard of care and the Summary of Product Characteristics during the study.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Adults greater than or equal to (≥) 18 years of age * Participants with solid tumors or lymphoproliferative disease * Participants receiving chemotherapy * Participants for whom erythropoietin is indicated for pre-study Hb level and observed anemic symptoms: Hb less than (\<) 11 g/dL or 6.83 millimoles per liter (mmol/L) * ECOG performance status of 0, 1, or 2 Exclusion Criteria: * Resistant hypertension * Acute chronic bleeding within 3 months prior to study * Iron deficiency that is unmanageable prior to study * Hypersensitivity to the active substance or any of the excipients of the product * Pregnant or breastfeeding women * Epoetin treatment within 6 months prior to study

Locations (42)

Unnamed facility

Outcomes

Primary Outcomes

Change in Hemoglobin (Hb) Level From Baseline to End of Treatment (EOT)

The change in Hb level from Baseline to the EOT visit at Month 4 was averaged among all participants and expressed in grams per liter (g/L).

Time frame: Baseline, Month 4

Secondary Outcomes

Percentage of Participants by Change in Eastern Cooperative Oncology Group (ECOG) Performance Status From Baseline to EOT

ECOG performance status was determined at Baseline and at the EOT visit at Month 4. The assessment used a 3-point scale, including scores of 0 (fully active/able to carry on all pre-disease activities without restriction), 1 (restricted in physically strenuous activity but ambulatory/able to carry out light or sedentary work), or 2 (ambulatory for more than 50% of waking hours and capable of all self care but unable to carry out any work activities). The traditional 6-point scale was not valid because only participants with a performance status of 0, 1, or 2 were eligible for the study. The percentage of participants by change in ECOG performance status was reported. For example, the percentage of participants with ECOG performance status of 0 at Baseline and 2 at EOT is shown in the table as "Baseline 0, EOT 2". Transition to a lower performance status indicates improved/increased independence.

Time frame: Baseline, Month 4

Percentage of Participants Who Required Blood Transfusions During the Study

The percentage of participants who required blood transfusions was reported at each assessment visit and was based on the 1-month period preceding the respective visit.

Time frame: Baseline to Month 1, Month 1 to 2, Month 2 to 3, Month 3 to 4

Data from ClinicalTrials.gov

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